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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528452Generated: October 25, 2026

Triphenylphosphine → (R)-2-(2,4,6-Trichloro-pyrimidin-5-yloxy)-propionic acid ethyl ester

https://huagongshe.com/reaction/528452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl (2R)-2-hydroxypropanoateHCID 637513—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant2,4,6-Trichloropyrimidin-5-olHCID 86667332—
Solvent1,4-DioxaneHCID 31275—
Product(R)-2-(2,4,6-Trichloro-pyrimidin-5-yloxy)-propionic acid ethyl esterHCID 8671173957.9%

Reaction Steps

A mixture of 2,4,6-trichloro-pyrimidin-5-ol (600 mg, 3.01 mmol), (R)-2-hydroxy-propionic acid ethyl ester (411 μL, 3.60 mmol), triphenylphosphine (906 mg, 3.45 mmol) and DIAD (678 μL, 3.45 mmol) in dioxane (5 mL) was stirred at RT for 18 hours before being concentrated in vacuo. The resulting residue was purified by column chromatography (SiO2, gradient 0-25% ethyl acetate in cyclohexane) affording (R)-2-(2,4,6-Trichloro-pyrimidin-5-yloxy)-propionic acid ethyl ester (522 mg, 52%). 1H NMR (400 MHz, CDCl3): δ 4.30-4.16 (2H, m), 4.12 (1H, q, J=7.14 Hz), 1.70 (3H, d, J=6.78 Hz), 1.29 (3H, t, J=7.19 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346817B2
Source datasetuspto-grants-2016_05
ORD IDord-4b434db0af1f41368810c66522e7fa17
Source noteuspto-grants-2016_05